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Blood transcriptomic signatures predict poor treatment outcomes in drug-susceptible pulmonary TB in Brazil
Simon C Mendelsohn1, Bruno B Andrade2, Mariana Araújo-Pereira2
1South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine and Division of Immunology, Department of Pathology, University of Cape Town, Anzio Road, Observatory, 7935, Cape Town, South Africa.
Background:
Non-sputum biomarkers to monitor tuberculosis (TB) treatment and predict poor outcomes are lacking. We evaluated host-blood transcriptomic signatures for treatment monitoring and prognosis (death, treatment failure, recurrence) in adults with pulmonary TB.
Methods:
Adults with culture-confirmed, drug-susceptible pulmonary TB were enrolled at five Brazilian sites. Whole-blood PAXgene samples were collected at baseline, month 2 (M2), and end of treatment (EoT). Treatment failure was defined as sputum culture positivity at month 5 or later. Participants were followed for 24 months from treatment initiation for clinical or microbiological TB recurrence. Unfavourable outcomes were matched ~1:3 to recurrence-free cure. Twenty-two published blood transcriptomic signatures were measured by microfluidic RT-qPCR and benchmarked against the WHO Target Product Profile (TPP) criteria.
Results:
We matched 263 participants with recurrence-free cure to 33 with treatment failure, 24 who died (TB/unknown cause), and 9 with recurrence. Signature scores generally declined from baseline to EoT. Multiple signatures predicted recurrence at baseline and M2 (AUC range 0.71-0.91), with waning performance at EoT (AUC range 0.42-0.89). Against the WHO TPP, 2/22 signatures met minimum criteria at baseline, 13/22 at M2, and none at EoT. Prediction of treatment failure was poor across timepoints (AUC <0.70). In contrast, Thompson5 and others at baseline predicted death during treatment or follow-up (AUC ≥0.80).
Conclusion:
Blood transcriptomic signatures tracked treatment response and predicted recurrence and death, meeting WHO TPP benchmarks at baseline and M2. These findings support prospective, biomarker-guided trials to individualise TB therapy-shortening regimens for early responders and intensifying care for high-risk patients.
Funding:
This work was supported by the U.S. National Institutes of Health, CRDF Global, and Departamento de Ciência e Tecnologia (DECIT) - Secretaria de Ciência e Tecnologia (SCTIE), Ministério da Saúde (MS), Brazil.
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